GB2206348A - 2-oxo-1(((substituted sulfonyl)amino)-carbonyl)azetidines - Google Patents

Description

A i 2 r 1.. " dc, 611 c 6 4t () M 1 - 2-OX0-1-[[(SUBSTIT=

SULF0NYL)AMIN01ICARBONnIAZETIDINES 1 Compounds having the formula R #2 P.,.NE c fig 2 GC249 Foreign p and pharmaceutically acceptable salts thereof, exhibit antibacterial activity. in formula 1, and throughout the specification, the symbols are as defined below..

is R is -A2 1 21 OE or R Aree '--LI I.

__A N 2 N R, is an acyl group derived from a carboxylic acid; R2 and R3 are the same or different and each is hydrogen, alkyl, alkenyl, alkynyl, cyclo alkyl, phenyl, substituted phenyl or a 4, 5, 6 or 7-membered heterocycle (hereinafter referred to as RX), or one of L2 and R 3 is hydrogen and the other is azido, halomethyl, dihalomethyl, tr:lhalomethyl, 1 1 1 is GC249 Foreign alkoxycarbonyl, 2-phenylethenyl, 2-phenylethynyl, carboxyl, -CE 2 X 1 [wherein X 1 is azido, amino (-NE 2), hydroxy, carboxyl, alkoxycarbonyl, alkanoylamino, phenylcarbonylamino, (substituted 5 phenyl)carbony,lamino, alkylsulfonyloxy, phenylsulfonyloxy, (substituted phenyl)sulfonyloxy, phenyl, substituted phenyl, cyano, -A-9-NX 6X711 -S-X2, or -0-X2 (wherein A, X2, X6 and X7 are as hereinafter defined)], -S-X, or -0-X2 [wherein X2 is alkyl, substituted alkyl, phenyl, substituted phenyl, phenylalkyl, (substituted phenyl)alkyl, alkanoyl, phenylalkanoyl, (substituted phenyl) alkanoyl, phenylcarbonyl, (substituted phenyl) X 3 carbonyl, or heteroarylcarbonyl], -0- -X4 or X 1 13 5 -S-P-X4 [wherein one of X3 and X4 is hydrogen and the other is hydrogen or alkyl, or X3 and X4 when taken together with the carbon atom to which they are attached form a cycloalkyl group; and X 5 is formyl, alkanoyl, phenylcarbonyl, (substituted phenyl)carbonyl, phenylalkylcarbonyl, (substituted 25 phenyl)alkylcarbonyl, carboxyl, alkoxycarbonyl, 0 Ii aminocarbonyl (NE 2 -C-), (substituted amino)- I carbonyl, or cyano, (-CEN)], or -A-C NX6 X7 [wherein A is -CE=CE-, -(CE2)m_91 -(CE 2)m-0-, -(CE2)m-NE-, or -CE 2-S-CE 2 -, m is 0, 1 or 2, and X6 and X7 are the same or different and each is hydrogen, alkyl, phenyl or substituted phenyl, or X6 is hydrogen and X7 is amino, substituted amino, alkanoylamino GC249 Foreign or alkoxy, or X 6 and X 7 when taken together with the nitrogen atom to which they are attached form a 4, 5, 6 or 7-membered heterocycle]; 0 11 A is -NE- or -NE-NE-C-; and IN-E-NE1 0 0 0 g ?1 1 A2 is a -NE- -CE2-' _ -NH-, ---NE-CH 2-0 0 -NI-I-C-CE--CE- or -CE=CE-; The above symbols (e.g., A and A 2) are used to represent groups of multiple atoms. These groups are inserted in the structural formulas shown herein in the order in which they are presented (i.e., from left to right). For example, if R is is 1 0 A JO"2 is -NE- and A is -NE-L the 2 kI 0 0 0 on 011 R group would be -NH n 0 t -NH N N Listed below are definitions of various terms 25 used to describe the g- lactams of this invention.

These definitions apply to the terms as they are used throughout the specification (unless they are otherwise limited in specific instances) either individually or as part of a larger group. The terms 11alkyll' and "alkoxyll refer to both straight and branched chain groups. Those groups having 1 to 10 carbon atoms are preferred. The terms Ilcycloalkyll' and Ilcycloalkenyll' refer to cycloalkyl and cycloalkenyl groups having 35 3, 4,5,6 or 7 carbon atoms.

1 GC249 Foreign The term "substituted alkyll' refers to alkyl groups substituted with one or more (preferably 1, 2 or 3) azido, amino (-NE2), halogen, hydroxy, carboxy, cyano, alkoxycarbonyl, aminocarbonyl, alkanoyloxy, alkoxy, phenyloxy. (substituted phenyl)oxy, mercapto, alkylthio, phenylthio, (substituted phenyl)thio, alkylsulfinyl, or alkyl sulfonyl groups.

The terms "alkanoylll, "alkenylll, and "alkynyll' refer to both straight and branched chain groups. Those groups having 2 to 10 carbon atoms are preferred.

The terms "halogen" and "halo" refer to fluorine, chlorine, bromine and iodine.

The term "substituted phenyl" refers to a phenyl group substituted with 1, 2 or 3 amino (-NB 2), halogen, hydroxyl, trifluoromethyl, alkyl (of 1 to 4 carbon atoms), alkoxy (of 1 to 4 carbon atoms), alkanoyloxy, aminocarbonyl, or carboxy groups.

The expression "a 4,5,6 or 7-membered heterocyclell (referred to as M, 11) refers to substituted and unsubstituted, aromatic and non-aromatic groups containing one or more (preferably 1, 2 or 3) nitrogen, oxygen or sulfur atoms. Exemplary substituents are oxo (=0), halogen, hydroxy, nitro, amino, cyano, trifluoro methyl, alkyl of 1 to 4 carbons, alkoxy of 1 to 4 carbons, alkylsulfonyl, phenyl, substituted phenyl, =N 2-furfurylideneamino (Loll -ICE and substituted alkyl groups (wherein the alkyl group has 1 to 4 carbons). one type of 114,5,6 or 7-membered heterocyclell is the 11heteroaryll' group.

The term 11heteroaryll' refers to those 4,5,6 or 7-membered heterocycles which are aromatic.

), benzylideneamino GC249 Foreign Exemplary heteroaryl groups are substituted and unsubstituted pyridinyl, furanyl, pyrrolyl, thienyl, 1,2,3triazolyl, 1,2,4-triazolyl, imidazolyl, thiazolyl, thiadiazolyl, pyrimidinyl, oxazolyl, triazinyl, and tetrazolyl. Exemplary nonaromatic heterocycles (i.e., fully or partially saturated heterocyclic groups) are substituted and unsubstituted azetidinyl, oxetanyl, thietanyl, piperidinyl, piperazinyl, imidazolidinyl, oxazolidinyl, pyrrolidinyl, tetrahydropyrimidinyl, dihydrothiazolyl and hexahydroazepinyl. Exemplary of the substituted 4,5,6 or 7-membered heterocycles are 1-alkyl-3-azetidinyl, 2-oxo-i-imidazolidinyl, 3alkylsulfonyl-2-oxo-l-imidazolidinyl, 3-benzylideneam:lno-2-oxo-l-imidazolidinyl, 3-alkyl-2-oxo-limidazolidinyl, 3-phenyl (or substituted phenyl)-2-oxo-l-imidazolidinyl, 3-berizyl-2oxo-l-imidazolidinyl, 3-(2-aminoethyl)2-oxo-l-imidazolidinyl, 3-amino-2-oxo-l- imidazolidinyl, 3-[(alkoxycarbonyl)amino]2-oxo-limidazolidinyl, 3-[2[(alkoxycarbonyl)amino]ethyl]-2-oxo-i-imidazolidinyl, 2-oxo-lpyrrolidinyl, 2-oxo-3-oxazolidinyl, 4-hydroxy-6methyl-2-pyrimidinyl, 2-oxo-lhexahydroazepinyl, 2-oxo-3-pyrrolidin:l, 2-oxo-3-tetrahydrofuranyl, 2,3dioxo-l-piperazinyl, 2,5-dioxol-piperazinyl, 4-alkyl-2,3-dioxo-lpiperazinyl, and 4-phenyl-2,3dioxo-l-piperazinyl.

The term "substituted amino" refers to a group having the formula -NX a X 9 wherein X. is hydrogen, alkyl, phenyl, substituted phenyl, phenylalkyl or (substituted phenyl)alkyl, and X. is alkyl, phenyl, substituted phenyl, phenylalkyl, (substituted phenyl)alkyl, hydroxy, cyano, alkoxy, phenylalkoxy, or amino (-NE,).

-20 GC249 Foreign The term "acyl" refers to all organic radicals derived from an organic acid (i.e., a carboxylic acid) by removal of the hydroxyl group. Certain acyl groups are, of course, preferred but this preference should not be viewed as a limitation of the scope of this invention. Exemplary acyl groups are those acyl groups which have been used in the past to acylate 0-1actam antibiotics including 6-aminopenicillanic acid and derivatives and 7-aminocephalosporanic acid and derivatives; see, for example, Cephalosporins and Penicillins, edited by Flynn, Academic Press (1972), German Offenlegungsschrift 2,716,677, published October 10, 1978, Belgian patent 867,994, published December 11, 1978, United States patent 4,152, 432, issued May 1, 1979, United States patent 3,971,778, issued July 27-, 1976, United States patent 4,172,199, issued Odtober 23, 1979, and British patent 1,348,894, published march 27, 1974. The portions of these references describing various acyl groups are incorporated hrein by reference. The following list of acyl groups is presented to further exemplify the term "acyl"; it should not be regarded as limiting tlat term. Exemplary acyl groups are: (a) Aliphatic groups having the formula 0 0 R.-c- wherein Ra is alkyl; cycloalkyl; alkoxy; alkenyl; j 1 0 is cycloalkenyl; cyclohexadienyl; or alkyl or alkenyl substituted with one or more halogen, cyano, nitro, amino, mercapto, alkylthio, or cyanomethylthio groups.

(b) Carbocyclic aromatic groups having the f ormula GC249 Foreign c R 0 Rb d 11 &( (CE 2 n-c_, R c P.b cl 0 it CH-C- C 1 qK e c 0 P.b d 11 cC CH 2 -0-C-91 c % tp-d 0 O-CE 2- 8- 11 is 0 P-b d fl 6d S-CH2-C- or R c %6p-d 0 -CE2-S-C- wherein n is 0, 1, 2 or 3; R b, Rc, and R a each is independently hydrogen, halogen, hydroxyl, nitro, amino, cyano, trifluoromethyl, alkyl of 1 to 4 carbon atoms, alkoxy of 1 to 4 carbon atoms or aminomethyl; and R e is amino, hydroxyl, carboxyl salt, protected carboxyl, formyloxy, sulfo salt, a sulfoamino, salt, azido, halogen, hydrazino, alkylhydrazino, phenylhydrazino, or 1(alkylthio)thioxomethyl]thio.

Preferred carbocyclic lromatic acyl groups' include those having the formula 0 It -.4 EO -0- CH2-C-01 0 R 2-C-P CR2NH2 GC249 Foiceign 1 0 is 0 0 11 ]E(>- H-C 1 R e a carboxyl salt or sulto salt) and GC249 Foreign (R e is preferably 11 CE-C- (R is preferably 0 e e a carboxyl salt or suifo salt).

(c) Beteroaromatic groups having the formula 0 Is E f- (CH 2)n-C-, 0 11 Rf CE-C- R e 0 11 Rt-O-CH 2-c- 0 tl 01 41 P.t-S-CH 2 -C- 0 0 11 It Rf -C-Cwherein n is 0, 1, 2 or 3; P-e is as defined above; and If is a substituted or unsubstituted 5-, 6- or 7-membered.heterocyclic ring containing 1,2,3 or 4 (preferably 1 or 2) nitrogen, oxygen sulfur atoms. Exemplary heterocyclic 0 0 GC249 Foreign rings are thienyl, furyl, pyrrolyl, pyridinyl, pyrazolyl, pyrazinyl, thiazolyl, pyrimidinyl, thladiazolyl and tetrazolyl. Exemplary substituents are halogen, hydroxyl, nitro, amino, protected amino, cyano, trifluoromethyl, alkyl of 1 to 4 carbon atoms, alkoxy of 1 to 4 carbon atoms, or 0 11 BOOC-CE-CH -0-C-NE 1 2 NE2 Preferred heteroaromatic acyl groups include those groups of the above formulas wherein.R. is 2-amino-4-thiazolyl, 2-amino-Shalo-4-thiazolyl, 4- aminopyrimidin-2-yl, 5-amino-1,2,4-thiadiazol-3-yl, 2-thienyl, 2-furanyl, or 6-aminopyridin-2-yl.

(d) [1(4-Substituted-2,3-dioxo-l-piperazinyl)carbonyl]aminolarylacety1 groups having the formula 0 0 -C-CE-NE-C-N N-Rh 1 R 9 oo wherein P. 9 is an aromatic group (including carbocyclic aromatics such as those of the formula Pb-62d and heteroaromatics as included within the definition of R f); and Rh is alkyl,. substituted k P GC249 Foreign alkyl (wherein the alkyl group is substituted with one or more halogen, cyano, nitro, amino or mercapto groups), arylmethyleneamino (i.e., -N=CE- R 9 wherein R 9 is as defined above), arylcarbonylamino (i.e., -NEIR 9 wherein R 9 is as defined above) or alkylcarbonylamino.

Preferred [J(4-substituted-2,3-dioxo- Ipiperazinyl)carbonyl]amino]arylacetyl groups include those wherein R. is ethyl, phenylmethyleneamino or 2- furylmethyleneamino.

(e) (Substituted oximino)arylacetyl groups having the formula is 1 wherein R 9 is as defined above and R i is hydrogen, alkyl, cycloalkyl, CE -(CE2) 1,2 or 31 2-pyrrazolylmethyl, \C/-cooE (2-oxo-3-pyrrolidinyl)methyl, alkylaminocarbonyl, arylaminocarbonyl (i.e., -C-IM-R 9 wherein R 9 is as defined above) or substituted alkyl (wherein the alkyl group is substituted with one or more ' halogen, cyano, nitro, amino, mercapto, alkylthio, aromatic group (as defined by R carboxyl (including salts thereof), amido, alkoxycarbonyl, phenylmethoxycarbonyl, diphe,.iylmethoxycarbonyl, hydroxyalkoxyphosphinyl, dihydroxyphosphinyl, hydroxy(phenylmethoxy)phos-ihin,vl, d:lalkoxyphosphinyl or tetrazolyl substituents).

0 1 GC249 Forerign in=lude those R 9 is thir-=olyl. Also z=c those is methyle ethylp 1-:za:bon. --1-nethlletnyl, the a 0 0 11 it 1 R 9 9 as de.-oined above and P. 2L5 b d RTr Ii - IRM ' \ so -r = --= -z= 2 ---2 ---2 J Ln lJ.

IZ= 0 2 -30 so -\=i---3' 0 X-1 1 a is 0 Preferred (acylamino)arylacetyl groups of the above formula include those groups wherein R j is amino or amido. Also preferred are those groups wherein R 9 is phenyl or 2-thienyl..(g) [1[3-Substituted-2-oxo-limidazolidinyllcarbonyllaminolarylacetyl groups having the formula 0 0 0 c -C-CE-NE-C-N N-R k 1 1 1 R CH 2-CE 2 wherein R 9 is as defined above and P-k is hydrogen, alkylsulfonyl, arylmethyleneamino (i.e., -N=CE-R wherein R is as defined 0 above), -C-Rm (wherein lm is hydrogen, alkyl or halogen substituted alkyl), aromatic group (as defined by R 9 above), alkyl or substituted alkyl (wherein the alkyl group is substituted with one or more halogen, cyano, nitro, amino or mercapto groups).

Preferred [[3-substituted-2-oxo-l-imidazolidinyllcarbonyllaminolarylacetyl groups of the above formula include those wherein R 9 is phenyl or 2-thienyl. Also preferred are those groups wherein Rk i!g hydrogen,, methyIsulfonyl, phenylmethyleneamino or 2furylmethyleneamino.

GC249 Fordign M GC249 Foreign The compounds of this invention form basic salts with various inorganic and organic bases which are also within the scope of this invention. Such salts include ammonium salts, alkali metal salts, alkaline earth metal salts, salts with organic bases, e.g., dicyclohexylamine, benzathine, N- methyl-D-glucamine, hydrabamine and the like. The pharmaccutically acceptable salts are preferred, although other salts are also useful, e.g., in isolating or purifying the product.

Some of the compounds of this invention may be crystallized or recrystallized from solvents containing water. In these cases, water of hydration may be formed. This invention contemplates stoichiometric hydrates as well as compounds containing variable amounts of water - that may be produced by processes such as lyophilization.

The P-lactams of formula I contain at least one chiral center---the carbon atom in the 3-position of the P-lactam nucleus to which the acylamino substituent ("R l-NE-11) is attached.

This invention is directed to those P-lactams which have been described above, wherein the stereochemistry at the chiral center in the 3-position of the P-lactam nucleus is the same as the configuration at the carbon atom in the 6-position of naturally occurring penicillins (e.g., penicillin G) and as the configuration at the carbon atom in the 7position of naturally occurring cephamycins (e.g., cephamycin C). Also included within the scope of this invention are racemic mixtures which contain the above-described p-lactams.

-is- GC249 Poreign The P-lactams of formula I, and pharmaceutically acceptable salts thereof, have activity against gram-positive and gram-negative organisms. The compounds of this invention can be used as agents to combat bacterial infections (including urinary tract infections and respiratory infections) in mammalian species, such as domesticated animals (e.g., dogs, cats, cows, horses, and the like) and humans.

Por combating bacterial infections in mAmmals, a compound of this invention can be administered to a mammal in need thereof in an amount of about 1.4 mg/kg/day to about 350 mg/kg/day, preferably about 14 mg/kg/day to about 100 mg/kg/day. All modes of administration which have been used in the past to deliver penicillins and cephalosporins to the site of infection are also contemplated for use with P-lactams of this invention. Such methods of administration include oral, intravenous, intra muscular, and as a suppository.

The p-lactams of formula 1 can be prepared from a 3-protected amino-2azetidinone having the formula II R t2 R4-NE CE---C-R 1 3 NE 1 In formula II, and throughout the specification, the symbol 11% 11 refers to an amino protecting group. These groups are well known in the field of p-lactam chemistry, and the particular group 35 chosen is not critical. Benzyloxycarbonyl,

1 GC249 Foreign trityl, and t-butoxycarbonyl are exemplary protecting groups. The reaction of a P-lactam of formula II with an isocyanate having the formula III O=C=N-SO 2-Y 1 wherein Y is a leaving group such as chlorine, yields the corresponding compound having the formula IV 12 R4 -NB 1 CE- C-R 1 1 3 / - -w-NE-SO 2-Y 0 The reaction is preferably run in an inert organic solvent, e.g., ethyl acetate, tetrahydrofuran, dimethoxyethane, dichloromethane, acetonitrile or mixtures of these solvents. Displacement of the leaving group 11Y11 with the desired group "R" can be accomplished using the appropriate nucleophile having the formula v RE, optionally in the presence of a base (e.g., triethylamine), and yields the corresponding compound having the formula vi P-2 R 4 -NE, L R 3 1 1--NE-SO 2-R 0 Alternatively, the displacement of the leaving group can be accomplished by reaction of a compound of formula IV with a protected form of a compound of formula V. Following the displacement reaction, the protecting groups can be removed using art-recognized techniques to yield a compound of formula VI.

1 GC249 Foreign Protected forms of a compound of formula V, and of all reactants described herein which contain a 3-hydroxy-4-pyridone moiety, include those compounds wherein the hydroxyl group is protected, those compounds wherein the hydroxyl group and the ring nitrogen are protected, and those compounds wherein both pyridone oxygens are protected. Exemplary protecting groups are silyl (e.g., trimethylsilyl), benzyl and acyl (e.g., acetyl). If silyl is used, later deprotection can be accomplished using hydrolysis or fluoride mediated cleavage. If benzyl is used, later deprotection can be accomplished by hydrogenolysis. If acyl is used, later deprotection can be accomplished by hydrolysis.

Deprotection of a compound of formula VI using conventional techniques yields the corresponding key intermediate having the formula II R NE 2 CE-R3 ,l-C-NE-SO -R 11 2 0 or a salt thereof. The particular deprotection reaction used will,'of course, depend on the protecting group ("R 4 11) present. If, for example, R4 is a t-butoxycarbonyl protecting group, deprotection can be accomplished by treatment of a compound of formula VI with acid (e.g., formic acid or trifluoroacetic acid). If, for example, R4 is a benzyloxycarbonyl protecting group, deprotection can be accomplished by catalytic hydrogenation of a compound of formula VI. Alternatively, the R 4 protecting group can be removed simultaneously with the -is- 10, GC249 Foreign other pyridone protecting groups immediately following the abovedescribed displacement reaction.

Well known acylation techniques can be used to convert an intermediate of formula VII to a corresponding product of formula I. Exemplary techniques include reaction of a compound of formula VII with a carboxylic acid (R 1OE), or corresponding carboxylic acid halide or carboxylic acid anhydride. The reaction with a carboxylic acid proceeds most readily in the presence of a carbodiimide such as dicyclohexylcarbodiimide and a substance capable of forming an active ester in situ such as N- hydroxybenzotriazole. in those instances where the acyl group (R 1) contains reactive functionality (such as amino or carboxyl groups) it may.be necessary to first protect those functional groups, then carry out the acylation reaction, and finally deprotect the resulting product.

An alternative procedure for preparing the compounds of formula I comprises first acylating (acylation techniques have been described above) a 3-amino-2-azetidinone having the formula VIII R g2 NE 3 to yield an intermediate having the formula IX R #2 R -NE 7 C-R 3 GC249 Foreign A -C-NE-SO 2-R activating group can be introduced in the 1-position of a compound of formula IX (using the procedures described above) to obtain the corresponding product of formula I. In those instances wherein the acyl side-chain "R 1 11 contains reactive functionality (such as amino groups), it may be necessary to first protect those functional groups, then carry out the 10 addition of the activating group in the 1-position, and finally deprotect the resulting product.

Still another synthesis for the preparation of compounds of formula I comprises the use of a 15 3-azido-2-azetidinone having the formula X N 3-_ V2 C-R 1 3 -NE 0 A --NE-SO 2-R activating group can be introduced in the 1-position of a compound of formula X (using the procedures described above) to obtain the corresponding compound having the formula xi R 12 N 3 L "E-C'-R 3 -N- -NESO -R o,/ A 2 Reduction of an intermediate of formula XI yields the corresponding intermediate having the formula 1 VII R 2 NE.,k2 C-R 1 3 -N-C-NE-SO -R.

N 2 0 GC249 Foreign The reduction can be accomplished by catalytic (e.g., palladium on charcoal or platinum oxide) hydrogenation or with reducing agents such as zinc or triphenylphosphine. As described above, from 10 these key intermediates (compounds of formula VII), using conventional acylation techniques, it is possible to prepare the products of formula I.

Alternatively, a 3-azido-2-azetidinone of formula X can be reduced to the corresponding 3-amino-2-azetidinone having the formula VIII R f2 NE 1 6-p. 3 1H.

The reduction can be accomplished by catalytic (e.g., palladium on charcoal or platinum oxide) hydrogenation or with reducing agents such as zinc or triphenylphosphine. A 3-amino-2-azetidinone of 25 formula VIII can be reacted as described above (i.e., first acylated and then treated as 0 described above to introduce a -9-NH-SO 2-R activating group in the 1-position) to yield the 30 products of formula I.

Still another synthesis for preparing the compounds of formula I wherein R2 and R 3 are each hydrogen utilizes a 6-acylaminopenicillanic acid having the formula L 1 XII R -NE 5 c (CH 3)2 T 1 GC249 Foreign or a salt thereof, as the starting material. By adapting procedures described in the literature, 3-acylamino-2-azetidinone can be obtained from the corresponding 6-acylaminopenicillanic acid of formula XII: see, for example, Chem. Soc. Special Publication No. 28, pg. 288 (1977), The Chemistry of Penicillins, Princeton University Press, pg. 257, and Synthesis, 494 (1977).

As described in the literature 6-acylaminopenicillanic acid, or a salt thereof, can be desulfurized to yield a compound having the formula XIII R l-NE CE-CE 1 2 ----'N-C -CH(CE3)2 COOE by reduction using Raney nickel. The reaction can be run in water under reflux conditions.

Replacement of the carboxyl group of a compound of formula XIII with an acetate group followed by hydrolysis yields the corresponding 3-acylamino2-azetidinone having the formula XIV R -NE 1 1 - CH ( 2 -NE Treatment of a compound of formula XIII with cupric acetate and lead tetraacetate in an organic 35 solvent (e.g., acetonitrile) replaces the carboxyl GC249 Foreign group with an acetate group. Hydrolysis of the resulting compound can be accomplished using potassium carbonate in the presence of sodium borohydride. 0 A -C-NE-SO 2 -R activating group can be introduced in the 1-position of a compound of formula XIV (yielding products of formula I wherein R 2 and R3 are each hydrogen) using the procedures described above.

Still another variation of the abovedescribed synthetic routes for preparing a compound of formula I wherein R2 and R3 are each hydrogen comprises first desulfurizing 6-amino- penicillanic acid, acylating the resulting compound to yield a compound of formula XIII and then proceeding as described above to obtain first a 3-acylamino-2-azetidinone of formula XIV and then a product of formula 1.

The azetidinones of formula 1 can also be prepared from amino acids having the formula xv OH Ik CE- 11,R2 OR R3 d The amino group is first protected (with a protecting group 11PA 11, e.g., 1-butoxycarbonyl).

The carboxyl group of the protected amino acid is then reacted with an amine having the formula XVI Z-0-NE2' wherein Z is alkyl, benzyl or triphenylmethyl, in the presence of a carbodiimide to yield a compound having the formula M I is GC249 Foreign OH R 4 -NE R 2 R 3 NE-0-Z The hydroxyl group of a compound of formula XVII converted to a leaving group (11OL) with a reagent, such as methanesulfonyl chloride or pyridineS03 complex.

The fully protected compound having the formula XVIII OL R4NH 1 011R2 CH-C-R 3 ""--NE-0-Z is is cyclized by treatment with base, e.g., potassium carbonate. The reaction is preferably carried out in an organic solvent or an organic solvent/water mixture under reflux conditions, and yields a compound having the formula xix R -NE R 4 N\ 2 \,,:,--c R 1 3 -N-0-Z Alternatively, cyclization of a compound of formula XVII can be accomplished without first converting the hydroxyl group to a leaving group. Treatment of a compound of formula XVII with triphenylphosphine and diethylazodicarboxylate, yields a compound of formula XIX.

Exemplary procedures for the conversion of a compound of formula XVIII to a compound of formula XIX are described in J. Amer. Chem. Soc., 102, 7026 (1980) and J. Org. Chem, 47, 5160 (1982).

GC249 Foreign Both of the methods disclosed above for ring closure of a compound of formula XVII result in the inversion of the stereochemistry at the carbon atom bearing the R2 and R3 substituents when R2 and R 3 are not the same.

Removal of the protecting group from the 1-position of an azetidinone of formula XIX can be accomplished via sodium reduction when Z is alkyl, and yields an intermediate having the formula 11 R4 -NE,,R2 NE (at least one of R2 and R3 is hydrogen). If Z is benzyl, catalytic (e.g., palladium on charcoal) hydrogenation will initially yield the corresponding N-hydroxy compound, which upon treatment with titanium trichloride yields an intermediate of formula Il. If Z is triphenylmethyl, formic acid or 70% acetic acid/water will initially yield the corresponding N-hydroxy compound. 0 A -9-NE-SO 2-R activating group can be introduced in the 1-position of a compound of formula II using the procedures described above, and the resulting compound can be deprotected and acylated.

The nucleophiles of formula V wherein R is 1 1 OE AM -Al- N A is -NE- and A is -NE-LI- 0 R 5JIA2 1 2 or -NE--CH 2_ can be prepared by reacting a GC249 Foreign nitroaniline compound having the formula XX N02AC)-N112 with an activated, suitably protected derivative of a carboxylic acid having the formula M no-C-(CE.5) N is 11 r E wherein r is 0 or 1, to yield, upon deprotection and reduction, the corresponding compound having the formula MI EO,i 1 CH) 0 --0-NE E 2 r- -NE 2 The nucleophiles of formula V wherein R is -A 1-0-A 2 H 19 1 1 OE 0 A 1 is -NH-NE-C and A 2 is NE-LI- or -NE-8-CE 2- can be prepared by reacting monoprotected hydrazine with a nitrobenzoic acid having the formula xxiii B00ot:::52 to obtain a compound having the formula xxiv 0 NO 2- -9-NE-NE-:Prot Q wherein Prot is a conventional amino protecting group. Reduction of a compound of formula XXIV to 35 yield the corresponding amino compound, followed GC249 Foreign by reaction with an activated, suitably protected carboxylic acid of formula XXI yields, upon deprotection, the corresponding compound having the formula xxv 0 g-NE NE-N EO-?N CH2) r-0 E2 E The nucleophiles of formula IV wherein R is 30- 1 1 on -A A 2 N A 1 is -NH-, and A 2 is -G-E 0 INE- or -CII-NE-CH 2- can be prepared by reacting a nitrobenzoic acid of formula XXIII with a suitably protected derivative of a compound having the formula xXVI OH NE -(CH AM 2 2 r N E to yield, after reduction and deprotection, the corresponding compound having the formula xXVII -A 0 N --C WE2 g-NE-(CH 2)rN H The nucleophiles of formula V wherein R is 1 W61 OH 0 -A,-Q-A 2 NI, A 1 is -NE-NH-6- and A 2 is E 0 0 -9-NE or -CLNE-CE 2can be prepared by reacting a dicarboxylic acid having the formula MI I I HO- with monoprotected hydrazine to obtain the corresponding compound having the formula X= Prot-NE-NE-C OR Reaction of a compound of formula X= with a suitably protected derivative of a compound of formula XXVI, followed by deprotection yields corresponding compound having the formula xxx 0C249 Foreign E2N-NE-C -NE-(CE2).r N E The nut] of formula V wherein R is 1] 0 -A A is -NB-, and A is -NE-C-CE=CH- 1 2 can be prepared by reacting a nitroaniline of formula XX with a suitably protected carboxyli.c acid having the formula X= OE HO-C-Cs--CE, N E to yield, after selective reduction (using, for example, sodium dithionate) and deprotection, the corresponding compound having the formula xxxii 0 11 NE -0-NE-C-CE=CH 2 E GC249 Foreign The nucleophiles of formula V wherein R is 0E 0 -NE-61-, and A2 is -A:,-&lig)-A 2 N A, is -NB E -NE-9-CE=CE- can be prepared by first reducing a compound of formula XXIV to the corresponding amino compound and then reacting that compound with a compound of formula X= to yield, upon deprotection, the corresponding compound having theformula xxxiii 0 -9-CE=M, 1 N, 1 NE2-NE-L -Q E The nucleophiles of formula V wherein R is 1 1 E 0 0 -A,-GA A is -NE- and A -g-NH-NH-g- 2 1 2 is can be prepared by first deprotecting a compound of formula XXIV and then reacting the deprotected compound with an activated, suitably protected derivative of a carboxylic acid having the formula xxxiv 0 EO to yield, upon reduction and deprotection, the corresponding compound having the formula xxxv 0 NE2-0j -NE-NE- N E is 1 1 1 t i i i GC249 Foreign The nucleophiles of formula V wherein R is 0 -A,-O-A 2 N A 1 is -NE-NE-9-, and A 2 is -C-NE-NE-C can be prepared by reacting a compound of formula XXIX with a suitably protected derivative of a compound having the formula xxxvi 0 NB 2-NE-9..' to yield, upon deprotection, the corresponding 15 compound having the formula MVII 0 0 1 1 OH NE 2-NE-L' -NH-NE-l-, X -oj H The nucleophiles of formula V wherein R is 1 1 N -Al-C-A, V A is -NE- and A is -CE=CE- 2 E 1 2 can be prepared by performing the Wittig reaction of a compound having the formula xxxviii NO 2 CCE=P---+)3 with a suitably protected derivative of an aldehyde having the formula M 1 ?1 1 EC,-1- E GC249 Foreign to yield, upon selective reduction of the ni tro group followed by depiotection, the corresponding compound having the formula XL NE2 The nucleophiles of formula V wherein R is 1 1 2m)-OE 0 -A 2 N, A 1 is -NE-NE-L' and A 2 is -CH=CE H can be prepared by performing the Wittig reaction of a protected derivative of a compound having the formula XLI 0 EO- -C CE=P-Q) 3 with a suitably protected derivative of an aldehyde of formula M to yield a protected derivative of the corresponding compound having the formula XLII 0 OR 'HO- ca--ca, WNT Deprotection of a compound of formula XLII, followed by reaction with a monoprotected hydrazine yields, upon deprotection, the corresponding compound having the formula XWII 1 NE2 -NE- CE--CE---- N E-0- H GC249 Foreign The nucleophiles of formula V wherein R is 1 1 0 -A N 1 A is -NE- and A NZ-9- 2 2 is 0 or -NE-C-CE 2 - can be prepared by reacting a diaminopyridine compound having the formula XLIV "R2 N NZ 2 with an activated, suitably protected derivative of a carboxylic acid of formula XXI to yield, upon deprotection, the corresponding compound having 15 the formula XW 0 E 0 (CE 2)r- -NE N NH The nucleophiles of formula V wherein R i 1 1 11 0 -A bN, A is -NE-NE-9 and A is - "2 2 0 -NE1 or -NE-C-CE- can be prepared by reacting an activated, suitably protected derivative of a compound of formula XXI with a compound having the formula XWI 0 Prot-NE-NE- 11 _ rx 2 to yield, upon deprotection, the corresponding compound having the formula XWI I GC249 Foreign 0 (CH) -c 2 r 11-M'úk,,Qj-NH-NH2 H The nucleophiles of formula V wherein R is 1 1 Ai-Q-A, 1 N A is --NE- 2 1 is -NE- and A 2 0 fl or -C-NE-CH 2- can be prepared by reacting a suitably protected derivative of a compound of formula XWI with a compound having the formula XWI I 1 0 is NE2-& 9-OE N to yield, after deprotection, the corresponding compound having the formula 1 L 0 OH N52-C--NH- (CE2 J r The nucleophiles of formula V wherein R is -A NW A A,2 is -NB-NH and A is N 2 7 11 -6-NE or -C-NE-CE- can be prepared by reacting a suitably protected derivative of a compound of formula XXVI with a compound having the formula n a 0 0 11 Prot-NE-NE-Ct Qo- 9-OE N 1 -33 GC249 Foreign to obtain, upon deprotection, the corresponding compound having the formula L E 2 N-NE-_eL- NB- (CH 2)-r cl 1 k-OK The nucleophiles of formula V wherein R is -A,-QJ-A A is -NB-, and A is 1 2 0 -NH-9-CE=CE- can be prepared by reacting a compound having the formula is LI NO 2-0-NE2 with a suitably protected derivative of a carboxylic acid of formula XXXI to yield, after selective reduction (using, for example, sodium dithionate) and deprotection, the corresponding compound having the formula LII i-ilir OE 0 NE 2,;-NE-C-CE= The nucleophiles of formula V wherein R is 0 __01 -A,-Q-A N 1 0 0 A 1 is -NE-NE-9-, and A 2 is -NB-9-CH=CE- can be prepared by reacting a compound of formula XWI with a suitably protected derivative of a compound of formula X= to yield, 0 upon deprotection, the corresponding compound having the formula LIII GC249 Foreign 0 0 NE2-NE- - NE-g-CH-CE2, _t nN The nucleophiles of formula V wherein R is 1 1 OE -A,-n-A IN, A is -NE- and A is N 2 E 1 2 is LIV 112 N_ -OE with an activated, suitably protected derivative of a carboxylic acid of formula XXXVI to yield, upon deprotection, the corresponding compound having the formula W 0 0 OH NE 2 Oj-NH-NE- Nr.

E The nucleophiles of formula V wherein R is 0 0 -A,-CA 2 N A 1 is -NE-NE-LI-, and A 2 is 0 NE-NE1 can be prepared by reacting a compound having the formula WI 0 0 11 Prot-NE-NE-1, -OR N 1 GC249 Foreign with an activated, suitably protected derivative of a compound of formula XXWI to yield, upon deprotection, the corresponding compound having the formula LVII 0 0 on 7\ -NB-NE NE2 4, The nucleophiles of formula v wherein R is 1 1 OE N 4N, A, is -NE- and A2 is -CE=CE- can be prepared by performing the Wittig reaction 15 of a compound having the formula LVIII Prot-NE-e=P--)3 with a suitably protected derivative of an 20 aldehyde of formula M to yield, upon deprotection, the corresponding compound having the formula LIX -OE The nucleophiles of formula V wherein R is cl-liroll 0 -Al-A N, A is -NE-NE-C- and A is N 2 E 1 2 -CE=CE can be prepared by performing the Wittig reaction of a protected derivative of a compound having the formula LX KO-g-eN)3 GC249 Foreign with a suitably protected derivative of an aldehyde of formula IXL to yield a protected derivative of the corresponding compound having the formula LXI 0 so 1 CE=CE N 1 1 OH E Deprotection of a compound of formula M, followed by reaction with monoprotected hydrazine yield, upon deprotection, the corresponding compound having the formula LXII 0 OH 11 ril 1 - is NE 2-NE-C--Ncll=CH]a Alternatively, the compounds of this invention can be prepared by first reacting a compound of formula IV with a compound having the formula LXIII E-A 1-RI-E-OE wherein R' iso- or in the presence of base or N-methyl-N-(trimethylsilyl)trifluoroacetamide to obtain a compound having the formula LX1V R 2 R-NE 4 CE--R3 N-C-NE-SO 2 A 1-Rl--OR.

A Reaction ofnd of formula UIV with a suitably protected derivative of a compound of the formula WV 0 GC249 Foreign OE E-A 1 2 0 11 wherein A' 2 is -NE-, -NE-CE 2- or -NB-NE-C-, yields upon deprotection and acylation, the corresponding product of formula I wherein A 2 i 0 0 0 if 11 11 -C-NE-CE..- or -C-NE-NE-C-.

0 5 -9-NS A compound of formula IV can also be reacted with a compound having the formula LXVI is E-A l-RINE-Prot in the presence of base or N-methyl-N-(trimethyl silyl)trifluoroacetamide to yield, upon deprotection, the corresponding compound having the formula LXVII R 12 CEC-R3 C -N-C-NE-SO 2-A l-R'-NE 2 Reaction of a compound of formula LXVII with a suitably protected derivative of a compound of the formula LM 11 0 OH 1 1 BO-All 2.& N A P 0 0 0 11 11 11 wherein All 2 is -C-, -C-M2- or -C-CE=CE-, yields upon deprotection and acylation, the corresponding 0 11 product of formula I wherein A 2 is -NE-C-r W GC249 Foreign -NE- -CE2- or -NHALCH--CH_.

The compounds described herein are pictured with the organic group 0 N E This group exists in a tautomeric equilibrium with a group of the formula H is OE -0 AQ N Depending on the additional substituent to the group, one form or the other will predominate. 20 Both forms are meant to be included herein. The following examples are specific embodiments of this invention.

-A 1 11....

GC249 Foreign Example 1 [3S(Z)]-2-[[[1-(2-Amino4-thiazolyl)-2-[[1-[[[[[4[[[(1,4-dihydro5-hydroxy-4-oxo-2pyridinyl)methyl)amino]carbonyl]phenyl]amino]sulfonyl]amino]carbonyl]5 2oxo-3-azetidinyl]amino]-2-oxoethylidene]aminoloxy]2-methylpropanoic acid, disodium salt A) N-[[1,4-Dihydro-4-oxo-S-(phenylmethoxy)-1(phenylinethyl)-2pyridinyllraethyl1-4-nitrobenzamide To a suspension of 10.7 g (0.03 mol) of N-[[1,4-dihydro-4-oxo-S-(phenylmethoxy)-1-(phenylmethyl)-2pyridinyl]methyl]amine in 100 ml of dichloromethane was added 8.96 ml of triethylamine (0.064 mol). A turbid brownish solution was formed, to which, with cooling, a solution of 5.57 g (0.03 mol) of 4-nitrobenzoyl chloride in 20 ml dichloromethane was added dropwise. The solution was stirred for 4 hours at room temperature, evaporated in vacuo and triturated with water to form 15.7 g of crude material, which was added to 100 ml of boiling ethanol. The pure compound crystallized from the boiling solution. Yield: 9.0 g of N-[[1,4-dihydro-4-oxo-S-(phenylmethoxy)-1-(phenylmethyl)2-pyridinyl]methyl]-4nitrobenzamide, melting point 188-190C. (DMSO-d 6): 8 = 4.37 (d, 2H); 5.06 (s, 2H); 5.18 (s, 2E); 6.20 (s, 1H); 6.91-7.30 (m, SH); 7.38 (m, SE); 7.72 (s, 1E); 8.04 (d, 2H); 8.30 (d, 2H); 19.30 (t, 1H) GC249 Foreign B) 4-Amino-N-[(1,4-dihydro-5-hydroxy-4-oxo-2Pyridinyl)methyllbenzamide, trifluoroacetate salt To a suspension of 8.5 g of 4-nitrobenzoyl chloride in 150 ml of dimethylformamide was added 6.93 ml of trifluoroacetic acid to form a solution. 4.5 Grams of palladium on charcoal (10%) was added and hydrogen was passed through the stirred suspension for two hours. After filtration, the filtrate was evaporated in vacuo and the residue triturated with ether to form 5.7 g of 4-amino-N[(1,4-dihydro-5-hydroxy-4oxo-2-pyridinyl)methyl]benzamide, trifluoroacetate salt. NMR (DMSO-d 6): 6 = 4.54 (m, 2H); 6.60 (d, 2H); 7.08 (s, 1H); 7.67 (d, 2H); 8.07 (s, 1R); 8.67-9.68 (m broad; 2 x NE, NE 2 OE = SE).

C) (S)-[1-[[[[[4-[[[(1,4-Dihydro-5-hydroxy-4-oxo2pyridinyl)methyl]amino]carbonyllphenyl]amino]sulfonyllamino]carbonyl]-2oxo-3-azetidinyl] carbamic acid, Rhenylmethyl ester To a suspension of 1.87 g of 4-amino-N[(1,4-dihydro-5-hydroxy-4-oxo-2pyridinyl)methyl]benzamide, trifluoroacetate salt (0.005 mol) in 20 ml of ethyl acetate was added 2.78 ml of Nmethyl-N-(trimethylsilyl)trifluoroacetamide (0.015 mol). After 10 minutes, a solution was formed (solution A). To a suspension of 1.1 g of (S)-3-[[(phenylmethoxy)carbonyl]amino]-2- azetidinone (0.005 mol) 30 in 20 ml of ethyl acetate was added 0.44 ml (0. 005 mol) of chlorosulfonylisocyanate to form a solution. The solution was stirred for 1 hour, then 2.09 ml of triethylamine (0.015 mol) and 20 ml of dichloromethane were added, with cooling, followed by solution A. The mixture was stirred overnight at k 1. 1 GC249 Foreign room temperature and evaporated in vacuo. The residue was dissolved in a mixture from acetone' and water and the pE of the mixture was adjusted to 6-6.5 by the addition of 2 N sodium hydroxide with cooling. After stirring for 2 hours, the acetone was removed in vacuo and the remaining aqueous phase was lyophilized. The crude sodium salt of (S)-[1-[[[[[4[[[(1,4-dihydro-5-hydroxy-4-oxo2pyridinyl)methyllamino]carbonyllphenyllamino)sulfonyl]amino]carbonyl]-2-oxo-3-azetidinyl] carbamic acid, phenylmethyl ester was purified by MPLC on XAD-2. The compound was eluted with water. The fractions containing pure compound (TLC) were collected, evaporated to a small volume and acidified to precipitate (S)-"[1-[[[[[4-[[[(1,4-dihydro-Shydroxy-4-oxo-2-pyridinyl)methyl]amino]carbonyl]phenyl]amino]sulfonyl]amino]carbonyl]-2-oxo-3- azetidinyl]carbamic acid, phenyImethyl ester. The precipitate was isolated by filtration.

Yield: 0.9 g of (S)-[1-[[[[[4-[[[(1,4-dihydro-Shydroxy-4-oxo-2-pyridinyl)methyl]amino]carbonyl]phenyl]amino]sulfonyl]amino)carbonyl]-2-oxo-3- azetidinyl]carbamic acid, phenyImethyl ester.

IR (KBr): 1775 (0-lactam) NMR (DMSO-d 6 + CF 3 COOR): 6 = 3.56 (dd, 1E); 3.80 (dd, 1E); 4.55 (s, M); 7.79 (dd, 1E); 5.00 (s, 2H); 7.15 (s, 1E); 7.30 (d, 2H); 7.32 (S, SE); 7.85 (d, M); 8.05 (s, 1H) D) (S)-3-Amino-N-[[[4-[[[(1,4-dihydro'5-hydroxy4-oxo-2-pyridinyl)methyl]amino]carbonyl]phenyl]amino]sulfonyl]-2oxo-l-azetidinecarboxamide, trifluoroacetate salt 1.2 Grams of (S)-[1-[[[[[4-[[[(1,4-dihydro5-hydroxy-4-oxo-2-pyridinyl)methyl]amino]carbonylI GC249 Foreign phenyl]amino]sulfonyl]amino]carbonyll-2-oxo-3azetidinyl] carbamic acid, phenylmethyl ester was added, at 100C, to a mixture of 5 ml of trifluoroacetic acid and 1 of ml thioanisole. The solution was stirred overnight at 1VC and evaporated in vacuo at room temperature. To the oily residue, 20 ml of ethyl acetate was added followed by 30 ml of ether. The precipitate was isolated by filtration. Yield: 1.1 g of crude (S)-3-aminoN-[[[4-[[[(1,4- dihydro-5-hydroxy-4-oxo-2pyridinyl)methyl]amino]carbonyl]phenyl]amino]sulfonyl]-2-oxo-iazetidinecarboxamide, 1,0-trifluoroacetate salt. IR (KBr): 1790 (p-lactam) E) [3S(Z)]-2-[[[1-(2-Amino-4-thiazolyl)-2-[[1[[[[[4-[[[(1,4-dihydro-5-hydroxy-4-oxo-2-pyridinyl)methyl]amino]carbonyl]phenyl]amino]sulfonyl]amino]carbonyl]-2-oxo-3-azetidinyl]aminol-2-oxoethylidenelamino]oxy]-2-methylpropanoic acid, diphenylmethyl ester To a suspension of 0.88 g (0.002 mol) of (Z)-2-amino-a-[[2-diphenylmethoxy)-1,1-dimethyl2-oxoetho:y]imino]-4-thiazoleacetic acid in 30 " ml of acetonitrile was added, at -300C, 0.84 ml of triethylamine (0.006 mol) followed by 0.44 ml of diphenyl chlorophosphate (0.002 mol) at the same temperature. The reaction mixture was stirred at -300C for 145 hours (solution A).

To a suspension of 1.1 g (0.002 mol) of (S)-3-amino-N-[[[4-[[[(1,4-dihydro-5-hydroxy-4oxo-2-pyridinyl)methyl]amino]carbonyl]phenyl]amino]sulfonyl]-2-oxo-i-azetidinecarboxamide, trifluoroacetate salt in 30 ml of ethyl acetate was added, at room temperature, 1.6 ml of bistrimethyl- silylacetamide (0.0066 mol).After stirring for 20 GC249 Foreign minutes, a clear solution was formed which was added to solution A at -30 to-25C. The reaction mixture was stirred at -100C for lh hours and at OOC for 1 hour and evaporated in vacup. The remaining syrup was triturated with ice water. The solid product was isolated by filtration. Yield: 1.7 g of crude [3S(Z)]-2-[[[1-(2-amino-4tbLiazolyl)-2-[[1-[[[[[4-1[[(1,4dihydro-5-hydroxy4-oxo-2-pyridinyl)methyl)amino]carbonyl)phenyl]amino]sulfonyl]amino]carbonyl]-2oxo-3-azetidinyllamino]-2oxoethylidene]amino]oxy]-2-methylpropanoic acid, diphenylmethyl ester. IR (KBr): 1776 (p-lactam) F) [3S(Z)]-2-[[[1-(2-Amino-4-thiazolyl)-2-[[1[[[[[4-[[[(1,4-dihydro-5-hydroxy-4-oxo-2pyridinyl)methyl]amino]carbonyl]phenyl]amino]sulfonyl]amino]-carbonyl]-2oxo-3-azetidinyl]aminol-2-oxoethylidene]aminoloxy]-2-methylpropanoic acid, disodium salt 1.7 Grams of [3S(Z)]-2-[[[1-(2-amino-4thiazolyl)-2-[[1[[[[[4-[[[(1,4-dihydro-5-hydroxy4-oxo-2pyridinyl)methyl]aminolcarbonyllphenyllamino]sulfonyl]araino]carbonyl]2oxo-3-azetidinyllamino]-2-oxoethylidene]aminoloxy]-2methylpropanoic acid, diphenylmethyl ester was added to a mixture of 17 ml of trifluoroacetic acid and 3.5 ml of anisole. The mixture was stirred for 1 hour at -100C. Ether was added at -100C to precipiate [3S(Z)]-2-[[[1-(2amino-4-thiazolyl)2-[[1-[[[[[4[[[(1,4-dihydro-5-hydroxy-4-oxo-2-pyridinyl)methyl]ino]tarbonyl]phenyl]amino]sulfonyl]amino]carbonyl] 2-oxo-3-azetidinyl]amino]-2-oxoethylidene]amino]oxy] 2-methylpropanoic acid, trifluoroacetate. Yield:

1.2 g of crude material. The crude compound was dissolved in a mixture of 30 ml of water and 20 ml 1 GC249 Foreign of acetone and the pE of the solution was adjusted to 5.5 - 6 by the addition of 2 N sodium hydroxide. The acetone was removed in vacuo and the remaining aqueous solution was lyophilized to yield 1.1 g of crude compound. The crude material was purified by chromatography on XAD-2 (elution with water). Yield: 0.22 g of pure [3S(Z)]-2-[[[1-(2-amino4thiazolyl)-2-[[1-[[[[[4-[[[(1,4-dihydro-5-hydroxy4-oxo-2pyridinyl)methyl]amino]carbonyllphenyllamino]sulfonyl]amino]carbonyl]-2-oxo-3-azetidinyllamino]-2-oxoethylidene]amino]oxy]-2-methylpropanoic acid, disodium salt. IR (KBr): 1770 (p-lactam) NMR (DMSO-d 6 + CF 3 COOE): 6 = 1.47 (s, W; 3. 70 (dd, M); 3.90 (dd, M); 4.57 (s, 2E); 5.07 (dd, M); 6.99 (s, 1E); 7.14 (s, M); 7.32 (d, 2E); 7.89 (d, 2H); 8.05 (s, 1E) Example 2 [3S(Z)]-2-[[[1-(2-Amino-4-thiazolyl)-2-[[1-[[[[ES-[[(1,4-dihydro-5-hydroxy-4-oxo-2-pyridinyl)carbonyl]amino]-2-pyridinyl]amino]sulfonyl]amino carbonyl]-2-oxo-3-azetidinyl]amino]-2-oxoethylidene]amino]oxy]-2-methylpropanoic acid, disodium salt I- A) N-(6-Amino-3-pyridinyl)-4,5-bis(phenylmethoxy)g=Ryridinecarboxamide To 7.28 g of 2,5-diaminopyridine, hydrochloride dissolved in 80 ml of dichlotomethane and 40 ml of acctonitrile were added 22.3 m-1 of triethylamine and at 0-5C a solution of 7.5 g of 4,57bis(phenyl methoxy)-2-pyridinecarboxylic acid chloride in ml of dichloromethane was added dropwise. After continuous stirring overnight, the precipitate was 1 1 is GC249 Foreign filtered off and washed with 20 ml of dichloromethane. The filtrate and the washed solution, both combined, were evaporated yielding 11.3 g of solid material. This was stirred with 100 ml of water, filtered off and dried. Purification by column chromatography on silica, eluting with ethyl acetate and then ethyl acetate/methanol (95:5) gave 5 g of N-(6- amino-3pyridiny,l)-4,5-bis(phenylmethoxy)-2-pyridinecarboxamide from fractions 138-215 (each 20 ml).

B) (S)-[1-[[[[[5[[[4,5-Bis(phenylmethoxy)-2pyridinyl]carbonyl]amino]-2pyridinyl]amino]sulfonyl] ino]carbonyl]-2-oxo-3-azetidinyl]carbamic acid, 1)henylmenyl ester 0.31 g of (S)-3-[[(phenylmethoxy)carbonyl]amino]-2-azetidinone and 0.12 mI, of chlorosulfonyl isocyanate were stirred for one hour at room temperature in 200 mI of ethyl acetate. At OOC, 0.59 ml of triethylaraine was added followed by 0.6 g of N-(6-amino-3-pyridinyl)-4,5-bis(phenyl- methoxy)-2-pyridinecarboxamide. After stirring overnight at room temperature and addition of ml dichloromethane crystals of crude (S)-[l [[[[[5-[[[4,5-bis(phenylmethoxy)-2-pyridinyl]carbonyl]amino]-2-pyridinyl]amino]sulfonyl]amino]carbonyl]-2-oxo-3azetidiny1]carbamic acid, phenyImethyl ester crystallized out. Purification of (S)-[1-[[[[[5-[[[4,5-bis(phenylmethoxy)2pyridinyl]carbonyl]amino]-2-pyridinyl]amino]sulfonyl]amino)carbonyl]-2-oxo-3-azetidiny.1]carbamic acid, phenylmethyl ester: column chromatography on EP-20 resin water/acetone gradient as cluent. Fractions 200-431 (water/acetone 6:4) contained 0.1 g of (S)-[l[[[[[5-[[[4,5-bis(phenylmetho.-.y)-2-pyridinyll- 9 GC249 Eoreign carbonyl]amino]-2-pyridinyl]amino]sulfonyl]ino]carbonyl]-2-oxo-3-azetidinyl]carbamic acid, phenylmethyl ester. Melting point 176-178C (dec.), white solid. IR (KBr): 1790cm-1 CO Plactam 'E-NMR (DMSO, 200 MHz): 8 = 3.12 - 3.75 (m, 2H); 4.73 (m, 1E); 5. 03 (s, 2E); 5.37 (s, 4H); 7.36 (m, 16E); 7.81 (2, 1H); 7.97 (d, 1E); 8.16 (d, 1H); 8.30 (s, IE); 8.63 (d, IE); 10.67 (s, 1E); ppm C) (S)-3-Amino-N-[[[5-[[1,4-dihydro-5-hydroxy-4oxo-2pyridinyl)carbonyl]amino]-2-pyridinyl]amino]sulfonyl]2-oxo-lazetidinecarboxamide, ditrifluoroacetate salt is 1.5 g of (S)-[1-[[[[[5-[[[4,5-bis(phenyl- methoxy)-2-pyridinyl]carbonyl]amino]-2pyridinyllamino]sulfonyl]amino]carbonyl]-2-oxo-3-azetidinyl]carbamic acid, phenylmethyl ester in 10 ml of trifluoroacetic acid and 2 ml of thioanisole were stirred for 18 hours at room temperature. 50 ml of ethyl acetate and 50 ml. of ether were added and a white precipitate of (S)-3-amino-N[[[5-[[1, 4dihydro-5-hydroxy-4-oxo-2-pyridinyl)carbonyllamino]-2pyridinyl]amino]sulfonyl]-2-oxo-l- azetidinecarboxamide, ditrifluoroacetate was obtained. IR (KBr): 1790cm-1 CO P-lactam- 1 D) [3S(Z)]-2-[[[1(2-Amino-4-thiazolyl)-2-[[1[[[[[5-[[(1;4-dihydro-S-hyclroxy-4-oxo-2-pyridinyl)carbonyl]amino]-2-pyridinyl]amino]sulfonyl]aminolcarbonyl]2-oxo-3-azetidinyl]amino]-2-oxoethylidene]amino]oxy]-2-methylpropanoic acid, disodium salt To 1.38 g of (Z)-2-amino-a-[[2-diphenylmethoxy 1,1-dimethyl-2-oxoethoxy]imino]-4-thiazoleacetic 1.

GC249 Foreign acid suspended in 30 ml of acetonitrile was added at -300C 1.34 ml of triethylamine followed by 0.71 ml of diphenylchlorophosphate in 10 ml of acetonitrile. After stirring for 1h hours at -300C, a solution of 2.1 g of silylated (S)-3-amino N-[[[5-[[1,4-dihydro-5-hydroxy-4-oxo-2-pyridinyl)carbonyllamino]-2-pyridinyl]amino]sulfonyl]-2- oxo-l-azetidinecarboxamide, ditrifluoroacetate salt in 50 ml of acetonitrile (obtained after stirring 2.1 g of (S)-3-amino-N-[[[5-[[1,4-dihydroShydroxy-4-oxo-2-pyridinyl)carbonyl]amino]-2pyridinyl)amino)sulfonyl]-2-oxo-l-azetidine- carboxamide, 2.0 trifluoroacetate with 3.16 ml of bistrimethylsilylacetamide for 30 minutes, evaporation and redissolving the residue in 50 ml of acetonitrile) was added dropwise (ca. 20 minutes). The mixture was stirred for 1 hour at - 100C and 1 hour at OOC. The solvent was distilled off in vacuo and the residue stirred in 100 ml of ice water and one drop of 2N hydrochloric acid for 1 hour. The precipitate was filtered off and washed with water. Yield: 3.1 g of crude [3S(Z)]2[[[-(2amino-4-thiazolyl)-2-[[1-[[[[[5-[[1,4-dihydro-Shydroxy-4-oxo-2pyridinyl)carbonyl]amino]-2-pyridinyl]amino]sulfonyllamino]carbonyl]-2-oxo-3-azetidinyl]amino]-2oxoethylidene]amino]oxy]-2-methylpropanoic acid, diphenylmethyl ester after drying. This material was dissolved in 50 ml of tetrahydrofuran and 1.5 g of sodium-2-ethylhexanoate was added, followed by 50 ml of ether. 1.9 g of precipitate of crude [3S(Z)]-2-[[[1(2-amino-4-thiazolyl)-2-[11-[[[[[5-[[(1,4-dihydro-Shydroxy-4-oxo-2pyridinyl)carbonyl)amino]-2-pyridinyl]amino]sulfonyl]amino]carbonyl]-2oxo-3-azetidiny1]amino]-2-oxoethylidene]amino]oxy]-2-methylpropanoic acid, diphenyl- GC249 Foreign methyl ester was isolated by filtration, beige solid. Purification of. this product by column chromatography on XAD-2 resin, water/acetonitrile gradient (9:1-6:4) and combination of appropriate fractions yielded 0.4 g of material. This material was dissolved in 10 mI, of trifluoroacetic acid and 2 mI, of anisole and stirred for 1 hour at -100C. After adding 40 ml of ether, 0.2 g of beige solid [3S(Z)]-2-[[[-(210 amino-4thiazolyl)-2-[[1-[[[[[5-[[1,4-dihydro-Shydroxy-4-oxo-2pyridinyl)carbonyl]amino]-2-pyridinyl]amino]sulfonyl]amino]carbonyl]-2oxo-3-azetidinyllamino]-2-oxoethylidene]amino]oxy]-2-methylpropanoic acid, trifluoroacetate salt was obtained (crude). is The crude material was dissolved in 5 ml of water + 3 inl of acetonitrile by adjusting the pE to 5.5 with sodium bicarbonate solution, filtering and chromatographing on a reverse phase Organogen column, water/acetonitrile (9:1) as eluent to 20 obtain 0.04 g of [3S(Z)]-2-[[[1-(2-amino-4-thiazolyl) 2-[[1-[[[[[5-[[(1,4dihydro-5-hydroxy-4-oxo-2pyridinyl)carbonyl]am'ino]2pyridinyl]amino]sulfonyl] aminolcarbonyl]-2oxo-3-azetidinyl]amino]-2oxoethylidene]amino]oxy]-2-methylpropanoic acid, disodium salt, melting point 2700-2900C (dec.). IE-MR (200 MEz): 6 = 1.27 (s, 6H); 3.53 (m, M); 3.80 (m, 1E); 4.82 (m, M); 6.67 (s, M); 7.08 (d, M); 8.29 (d, 1E); ppm IR (KBr): 1790cm-1 CO g-lactam 1 A.

Claims (25)

1. A compound having the formula R,-NE P-

2 P'

3 "E- c A-g-NE-SO 2-R or such a compound in pharmaceutically acceptable salt form, wherein 2 or N. 2 RI is an acyl group derived from a carboxylic acid; GC249 Foreign R2 and R3 are the same or different and each is hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl, phenyl, substituted phenyl or a 4, 5, 6 or 7- membered heterocycle or one of R 2 and R 3 is hydrogen and the other is azido, halomethyl, dihalomethyl, trihalomethyl, alkoxycarbonyl,. 2phenylethenyl, 2-phenylethynyl, carboxyl, X f3 13 -C%X11 -S-X21 -0-XV -0-C-X4 -S-C-X4 or 0 X -A-9-NX 6X7; X, is azido, amino, hydroxy, carboxyl, alkoxycarbonyl, alkanoylamino, phenylcarbonylamino, (substituted phenyl)carbonylamino, alkylsulfonyloxy. phenylsulfonyloxy, (substituted phenyl)sulfonyloxy, phenyl,'substituted phenyl, cyano, -so- GC249 Foreign -AINX J7' -S-X2, or -0-X2 X2 is alkyl, substituted alkyl, phenyl, substituted phenyl, phenylalkyl, (substituted phenyl)alkyl, alkanoyl, phenylalkanoyl, (substituted phenyl)alkanoyl, phenylcarbonyl, (substituted phenyl)carbonyl, or heteroarylcarbonyl; one of X3 and X,, is hydrogen and the other is hydrogen or alkyl, or X3 and X4 when taken together with the carbon atom to which they are attached form a cycloalkyl group; X5 is forMY1, alkanoyl, phenylcarbonyl, (substituted phenyl)carbonyl, phenylalkylcarbonyl, (substituted phenyl)alkylcarbonyl, carboxyl, alkoxycarbonyl, aminocarbonyl, (substituted no)carbonyl, or cyano; X. and X7 are the same or different and each is hydrogen, alkyl, phenyl or substituted phenyl, or X 6 is hydrogen and X7 is amino, substituted ino, alkanoylamino or alkoxy, or X 6 and X7 when taken together with the nitrogen atom to which they are attached form a 4, 5, 6 or 7membered heterocycle; A is -M--CE-, ( CYza-' _(CE2)m_001 _(CE2)m-NE or -CE2-S-CE2_; m is 0, 1 or 2; 1 A, is -NE- or -NE-NE-6-; and j 0 0 0 A2 is -NE -1 -NE-g-CE2-1 0 -NE-A-CE=CE- or -CE--CE- 0 1 9 GC249 Foreign 2. A compound in accordance with claim 1 1 1 on wherein R is -A,- 5 I@A2 ja 3. A compound in accordance with claim 1 wherein R is -Arp 2 E

4. A compound in accordance with claim 2 whereln A., is -NE-.

5. A compound in accordance with claim 3 wherein A, is -NE-.

6. A compound in accordance with claim 2 0 wherein A 1 is -NE-NEA_.

7. A compound in accordance with claim 3 wherein A, is -NE-NE-C-.

8. A compound in accordance with claim 2 0 wherein A 2 is -NEA_.

9. A compound in accordance with claim 2 0 wherein A 2 is -NBA-CE2--

10. A compound in accordance with claim 2 0 wherein A. is -9-NE-.

11. A compound in accordance with claim 2 wherein A 2 is INE-CE2--

12. A compound in accordance with claim 2 0 0 wherein A. fi- , is -C NE-NE-9-r GC249 Foreign

13. A compound in accordance with claim 2 wherein A 2 is

14. A compound in accordance with claim 2 wherein A 2 is -M--CH_.

15. A compound in accordance with claim 3 wherein A 2 'S -NB- L -

16. A compound in accordance with claim 3 0 wherein A 2 is -NE-g-CE2_.

17. A compound in accordance with claim 3 wherein A 2 'S

18. A compound in accordance with claim 3 1 ? wherein A 2 is -C-NE-ICE 2

19. A compound in accordance with claim 3 0 0 wherein A 2 is -c NB-NE-L

20. A compound in accordance with claim 0 wherein A 2 is -NE-9-CECE-.

21. A compound in accordance with claim 3 wherein A 2 is -M--CE-.

22. A compound in accordance with claim 1 0 wherein PI, is -LC=N-O-R. and R is 2-amino-4- thiazolyl az methyl, ethyl, carboxymethyl, 1-carboxy-l-methylethyl, 1-carboxy-l-ethyl, or CE -(CE \2 ' 2 S -COOS, wherein s is 1, 2, or 3.

3 1 GC249 Foreign

23. A compound in accordance with claim 1 0 wherein R 1 is -9-C=N-O-Rif R 9 is 2-amino-4-thiazolyl- 1 9 - and R i is ca ethyl, 1-carboxy-l-methylethyl, k2 ( 02 s :1C 0 1-carboxy-l-ethyl or -c- E, wherein s is 1, 2 or 3.

24. The compound in accordance with claim 1, [3S(Z)]-2-[[[1-(2-amino-4thiazolyl)-2-[[1-[[[[[4 [[[(1,4-dihydro-5-hydroxy-4-oxo-2pyridinyl)methyl]amino]carbonyl]phenyl]amino]sulfonyl]amino]carbonyl] 2oxo-3-azetid:Lnyl]am:Lno]-2-oxoethylidene]am:Lno]oxy] 2-methylpropanoic acid, or a pharmaceutically acceptable salt thereof.

25. The compound in accordance with claim 1, [3S(Z)]-2-[[[1-(2-amino4thiazolyl)-2-[[1-[[[[ [5-[[(1,4-dihydro-5-hydroxy-4-oxo-2pyridinyl)carbonyllamino]-2-pyridinyl]amino]sulfonyl]amino] carbonyl]-2oxo-3-azetidinyl]amino]-2-oxoethylidene]amino]oxy]-2-methylpropanoic acid, or a pharmaceutically acceptable salt thereof.

Published 19813 at Une Patent Office, State House, 66.71 Righ Holborn, London WC1R 4TP. Parther copies may be obtained from The Patent office, technicues ltd, St Maiy Cray, Kent. Con, 1'87 technicues ltd, St Maiy Cray, 11ert. Uon, 1't37.